FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SEARE BIOMEDICAL PECTORALIS IMPLANT

K Number: K982762 · Decision Sep 30, 1998
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
7
Applicant Total
8
Review Days
55

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Basic Information

Device Name
SEARE BIOMEDICAL PECTORALIS IMPLANT
K Number
K982762
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3620
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Seare Biomedical Corp.
Date Received
August 6, 1998
Decision Date
September 30, 1998
Product Code
MIC
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MIC Implant, Muscle, Pectoralis

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MIC), ordered by most recent decision date.

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Other Clearances by Seare Biomedical Corp.

K Number Device Name
K983792 SEARE BIOMEDICAL SILICONE TISSUE EXPANDER
K983630 SEARE BIOMEDICAL SILICONE RODS
K983043 SEARE BIOMEDICAL SILICONE BLOCK
K982752 SEARE BIOMEDICAL CHIN IMPLANTS
K982753 SEARE BIOMEDICAL NASAL IMPLANTS
K982763 SEARE BIOMEDICAL MALAR IMPLANTS
K983041 SEARE BIOMEDICAL SILICONE SHEETING